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Acta Ophthalmologica Scandinavica|December 1, 1996
Full-field electroretinograms in a family with Mohr-Tranebjaerg syndromeV Ponjavic, S Andreasson, L Tranebjaerg, et al.
American Journal of Medical Genetics|March 7, 2000
Jervell and Lange-Nielsen syndrome: a Norwegian perspectiveL Tranebjaerg, J Bathen, J Tyson, et al.
European Journal of Pediatrics|October 3, 2000
Immunodeficiency in alpha-mannosidosis: a matched case-control study on immunoglobulins, complement factors, receptor density, phagocytosis and intracellular killing in leucocytesD Malm, D S Halvorsen, L Tranebjaerg, et al.
Human Genetics|May 1, 1997
The tricho-rhino-phalangeal syndromes: frequency and parental origin of 8q deletionsJ Nardmann, L Tranebjaerg, B Horsthemke, et al.
American Journal of Medical Genetics|July 12, 1996
Inheritance of skewed X chromosome inactivation in a large family with an X-linked recessive deafness syndromeK H Orstavik, R E Orstavik, K Eiklid, et al.
Hereditas|January 1, 1989
Localization in man of fifteen DNA sequences within the chromosome segment 13q12-q22K Arheden, U Tantravahi, N Tommerup, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|February 20, 1995
[Alpha-mannosidosis]D Malm, O K Tollersrud, L Tranebjaerg, et al.
Annales De Genetique|January 1, 1984
Clinical and cytogenetic studies in a large (4;8) translocation family with pre- and postnatal Wolf syndromeL Tranebjaerg, A Petersen, K Hove, et al.
Clinical Genetics|August 1, 1987
Partial trisomy 3q syndrome inherited from familial t(3;9)(q26.1; p23)L Tranebjaerg, U B Baekmark, M Dyhr-Nielsen, et al.
European Journal of Human Genetics : EJHG|February 13, 2002
Spectrum of CLCN1 mutations in patients with myotonia congenita in Northern ScandinaviaC Sun, L Tranebjaerg, T Torbergsen, et al.
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